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. 2016 Oct;22(10):1500–1509. doi: 10.1261/rna.057455.116

FIGURE 3.

FIGURE 3.

Trl1 titration. Reaction mixtures (20 µL) containing 50 mM Tris–HCl (pH 7.5), 2 mM DTT, 10 mM MgCl2, 100 µM ATP, 100 µM GTP, 20 nM 20-mer HORNA>p (depicted at the bottom), and 0.5. 1, 2, 5, 10, 20, 50, or 100 nM Trl1 (from left to right in each titration series) were incubated for 30 min at 22°C. Trl1 was omitted from control reactions in lanes (–). The products were analyzed by urea–PAGE. An autoradiograph of the gel is shown. The positions and identities of the HORNA>p substrate (*), 5′-phosphorylated kinase product (5′-P), and the ligation products (circle and multimers) are indicated.